Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72653706
ABCC6
0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs28933981
TTR
0.807 0.200 18 31598647 missense variant C/T snv 1.5E-03 1.7E-03 8
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs34203073
AGGF1
1.000 0.040 5 77035624 missense variant G/A snv 1.0E-02 9.9E-03 2
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1800458
TTR
0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 5
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs6809699
P2RY12 ; MED12L
1.000 0.080 3 151338810 synonymous variant A/C snv 0.87 0.88 2
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18